Roche
receives blood cancer drug blow after Gazyva trial fails to meet
endpoint
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[July 18, 2016]
ZURICH (Reuters) - Swiss drugmaker
Roche said trials showed its new blood cancer drug Gazyva failed to
deliver significant improvements over an older medicine in people with
an aggressive type of blood cancer, a blow in its fight against
competition from biosimilars.
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Gazyva did not significantly reduce the risk of disease worsening or
death for people with previously untreated diffuse large B-cell
lymphoma, over current drug Rituxan in a phase III GOYA study, Roche
said on Monday.
Diffuse large B-cell lymphoma is the most common form of
non-Hodgkin's lymphoma. An estimated 25,000 new U.S. cases of the
aggressive blood cancer, and 10,000 deaths from it, are seen each
year.
"Two previous studies showed Gazyva/Gazyvaro helped people with
previously untreated follicular lymphoma or chronic lymphocytic
leukemia live longer without their disease worsening compared to
MabThera/Rituxan, when each was combined with chemotherapy," Roche's
Chief Medical Officer Sandra Horning said.
"We were hopeful we could show a similar result for people with
diffuse large B-cell lymphoma and once again improve on the standard
of care."
The study included 1,418 previously untreated patients.
Clinical trials with the new drug are important in deciding how well
the Swiss company is placed to fend off cheaper competition from
so-called biosimilar copies of Rituxan, which are likely to hit the
market in the next couple of years.
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Strong results with Gazyva mean Roche can argue that its new drug
delivers better results for patients, even if it is more expensive
than biosimilars.
Roche's shares were boosted in May after Gazyva proved significantly
better than Rituxan at delaying disease progression in people with
previously untreated follicular lymphoma, and Chief Executive
Severin Schwan said he could "sleep better" after the win for Roche.
(Reporting by Brenna Hughes Neghaiwi; Editing by Biju Dwarakanath)
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